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Isolation and Chemical Characterization of a Capsular Polysaccharide Antigen Shared by Clinical Isolates of Enterococcus faecalis and Vancomycin-Resistant Enterococcus faecium

机译:粪肠球菌和耐万古霉素肠球菌临床分离株共有的荚膜多糖抗原的分离和化学表征

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摘要

Enterococci are a common cause of serious infections, especially in newborns, severely immunocompromised patients, and patients requiring intensive care. To characterize enterococcal surface antigens that are targets of opsonic antibodies, rabbits were immunized with various gentamicin-killed Enterococcus faecalis strains, and immune sera were tested in an opsonophagocytic assay against a selection of clinical isolates. Serum raised against one strain killed the homologous strain (12030) at a dilution of 1:5,120 and mediated opsonic killing of 33% of all strains tested. In addition, this serum killed two (28%) of seven vancomycin-resistant Enterococcus faecium strains. Adsorption of sera with the homologous strain eliminated killing activity. The adsorbing antigens were resistant to treatment with proteinase K and to boiling for 1 h, but were susceptible to treatment with sodium periodate, indicating that the antigen inducing opsonic activity is a polysaccharide. Antibodies in immune rabbit sera reacted with a capsule-like structure visualized by electron microscopy both on the homologous E. faecalis strain and on a vancomycin-resistant E. faecium strain. The capsular polysaccharides from E. faecalis 12030 and E. faecium 838970 were purified, and chemical and structural analyses indicated they were identical glycerol teichoic acid-like molecules with a carbohydrate backbone structure of 6-α-d-glucose-1-2 glycerol-3-PO4 with substitution on carbon 2 of the glucose with an α-2-1-d-glucose residue. The purified antigen adsorbed opsonic killing activity from immune rabbit sera and elicited high titers of antibodies (when used to immunize rabbits) that both mediated opsonic killing of bacteria and bound to a capsule-like structure visualized by electron microscopy. These results indicate that approximately one-third of a sample of 15 E. faecalis strains and 7 vancomycin-resistant E. faecium strains possess shared capsular polysaccharides that are targets of opsonophagocytic antibodies and therefore are potential vaccine candidates.
机译:肠球菌是导致严重感染的常见原因,尤其是在新生儿,严重免疫功能低下的患者以及需要重症监护的患者中。为了表征作为调渗抗体靶标的肠球菌表面抗原,用庆大霉素杀死的粪肠球菌菌株对兔进行免疫,并在调理吞噬试验中针对选择的临床分离物测试免疫血清。针对一种菌株产生的血清以1:5,120的稀释度杀死了同源菌株(12030),并且介导的调理性杀死所有测试菌株的33%。另外,该血清杀死了七个耐万古霉素的粪肠球菌菌株中的两个(28%)。用同源菌株吸附血清消除了杀伤活性。吸附的抗原对蛋白酶K的处理和煮沸1小时具有抗性,但对高碘酸钠的处理很敏感,表明诱导调理活性的抗原是多糖。免疫兔血清中的抗体与通过电子显微镜观察的荚膜样结构在同源的屎肠球菌菌株和耐万古霉素的屎肠球菌菌株上反应。纯化了屎肠球菌12030和屎肠球菌838970的荚膜多糖,化学和结构分析表明它们是相同的甘油海胆酸样分子,具有6-α-d-葡萄糖-1-2甘油-的碳水化合物主链结构。 3-PO4,在葡萄糖的碳2上被α-2-1-d-葡萄糖残基取代。纯化的抗原从免疫兔血清中吸附了调理光杀死活性,并引发了高滴度的抗体(当用于对兔进行免疫时),它们介导细菌的调理光杀死,并结合到电子显微镜观察的胶囊状结构上。这些结果表明,在15个粪肠球菌菌株和7个耐万古霉素的粪肠球菌菌株的样品中,约有三分之一具有共享的荚膜多糖,它们是调理吞噬细胞抗体的靶标,因此是潜在的候选疫苗。

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